Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion> ?p ?o ?g. }
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- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion type Assertion NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_head.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion evidence source_evidence_curated NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion SIO_000772 23561846 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion wasDerivedFrom uniprot-2016 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion wasGeneratedBy ECO_0000218 NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.